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Loss of Chromosome 9q

Known as: del(9q) 
A cytogenetic abnormality that refers to deletion of part of the long arm of chromosome 9. It is associated with the development of acute myeloid… Expand
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
SF3B1 mutations in primary myelofibrosis: clinical, histopathology and genetic correlates among 155 patients 
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Highly Cited
2010
Highly Cited
2010
PURPOSE Because cytogenetic data are essential for risk stratification of childhood acute myeloid leukemia (AML), the impact of… Expand
Highly Cited
2009
Highly Cited
2009
Acute myeloid leukemia (AML) with mutated NPM1 usually carries normal karyotype (NK), but it may harbor chromosomal aberrations… Expand
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Highly Cited
2008
Highly Cited
2008
Deletions on chromosome 9q are seen in a subset of acute myeloid leukemia (AML) cases and are specifically associated with t(8;21… Expand
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Highly Cited
2007
Highly Cited
2007
We have generated a large, unique database that includes morphologic, clinical, cytogenetic, and follow-up data from 2124… Expand
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Highly Cited
2006
Highly Cited
2006
To better understand the spectrum of adult acute myeloid leukaemia (AML) associated with core binding factor (CBF) translocations… Expand
2005
2005
To assess the prevalence of mutations in the CEBPA gene, which encodes the myeloid transcription factor CEBPA in specific… Expand
Highly Cited
1998
Highly Cited
1998
Cytogenetics is considered one of the most valuable prognostic determinants in acute myeloid leukemia (AML). However, many… Expand
Highly Cited
1996
Highly Cited
1996
The translocation t(8;21)(q22;q22) occurs in 6 to 12 percent of patients with AML, and usually predicts a good response to… Expand
Highly Cited
1986
Highly Cited
1986
Information was retrieved from a computer-based data bank about additional chromosome aberrations in patients with acute… Expand